6-Hour Virtual Seminar on The EU Clinical Trial Regulation - EU Filings & Registrations

This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics).

The course also covers recent updates on EU-GCP associated with the new regulatory framework and highlights the new EU Pharmacovigilance Directive, as it relates to studies and helpful tips for working with European regulators.

The seminar covers the impending changes coming with the EU Parliament's passage of the EU Clinical Trial Regulation, which will affect all trials conducted across the EU [new and ongoing].

This course also covers the various licensing methods (for Drugs, Biologics & Combination Products) by which applicants can file for product licenses (Marketing Authorizations) in one or multiple Member States [and EEA], as well as fully across all Member States of the European Union.

This course specifically outlines and discusses the structure of the regulatory agencies at the EU level and across the specific Member States. Course content will explain which procedures are available for which products and then will follow the license processing steps for each pathway.

Learning Objectives:
Attendees will leave the Course clearly understanding the requirements under the current Regulations. In addition, this course has been updated to provide participants with competitive insight into:

• How the EU and individual countries within Europe interact
• Which registration procedure to use
• How regulations affect product development strategies
• Understanding the concerns/issues of European Regulatory Personnel
• How to negotiate with the regulators
• Information necessary for effective submissions
• Strategies for streamlining the registration application process for faster approval
• The advantages and disadvantages of various registration procedures
• How to efficiently initiate trials, the first patient, first visit
• How to link the strategy of Country Selection to an ultimate EU registration pathway
• How to stay compliant What can make the difference in your data passing Regulatory scrutiny
• Related area-GCP and PV-reporting updates
• Impending Changes of the EU Clinical Trial Regulation and Timing for Implementation

• Overview of the EU and EU Regulatory Structure
• Overview of the previous EU Clinical Trial Directive
• Impending Changes of the EU Clinical Trial Regulation
• Clinical Trials in the EU
  • Phases of a clinical trial
  • Start-Up and Application Processes
  • Ethics Committee and Competent Authority Review Process
  • Trial Protocol and Management
  • GCP and GMP Compliance
  • Labeling Requirements
  • Fees
• End of a Clinical Trial
• How Changes in the New Clinical Trial Regulation will affect Sponsors

• EU Agency Regulatory Structure
• Registration Options
• Company Strategy - Linking Clinical Trials & Marketing Authorization Applications
• Balancing Strategy and Long-Term Regulatory Cost & Maintenance
• Registration Procedures

• Mutual Recognition Procedure
• Centralized Procedure
• Generics, Orphan Drugs, Biologics, and Combination Products
• Cessing License Variations
• Changes Concerning Manufacturing / Formulation Aspects (Product & Process)
• Labeling & Packaging Leaflet Requirements

• Scope
• Check-in Procedure
• Consultation
• Industry's Ability to Impact - Involvement & Timing
• Standing Committee Participation
• Favorable Standing Committee Opinion
• Non-Favorable Opinion - Process & Timing

• International, Regional, and Local laws applicable for each European Union Nation

• Legislative Process
• Objectives of the Rules Governing Medicinal Procedures
• Regulatory Framework
• New Products, Requirements, & Procedures

• Compare/Contrast EMA and the FDA procedures

• Effective Monitoring Activity
• Association vs. Individual Company Involvement & Intervention
• The Regulatory Negotiation Process
• Effective Approaches
• The Do's and Don'ts of Regulatory Involvement

• Business Management
• Project Team Members
• Legal Team Members
• Clinical Operations Staff
• Quality Assurance, Monitors, CRAs
• Regulatory Affairs
• Investigators & Site Study Staff
• CROs, Consultants, Insurers